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eXIST with matrix-associated proteins
被引:14
|作者:
Nakagawa, Shinichi
[1
,2
]
Prasanth, Kannanganattu V.
[3
]
机构:
[1] RIKEN, Adv Res Inst, RNA Biol Lab, Wako, Saitama 3510198, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Univ Illinois, Chem & Life Sci Lab, Dept Cell & Dev Biol, Urbana, IL 61801 USA
关键词:
X-CHROMOSOME INACTIVATION;
ATTACHMENT REGION DNA;
LONG NONCODING RNAS;
XIST RNA;
NUCLEAR-MATRIX;
BINDING-PROTEIN;
GENE-EXPRESSION;
IN-VIVO;
SAF-A;
HNRNP U;
D O I:
10.1016/j.tcb.2011.02.001
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
X-chromosome inactivation has long served as an experimental model system for understanding the epigenetic regulation of gene expression. Central to this phenomenon is the long, non-coding RNA Xist that is specifically expressed from the inactive X chromosome and spreads along the entire length of the chromosome in cis. Recently, two of the proteins originally identified as components of the nuclear scaffold/matrix (S/MAR-associated proteins) have been shown to control the principal features of X-chromosome inactivation; specifically, context-dependent competency and the chromosome-wide association of Xist RNA. These findings implicate the involvement of nuclear S/MAR-associated proteins in the organization of epigenetic machinery. Here, we describe a model for the functional role of S/MAR-associated proteins in the regulation of key epigenetic processes.
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页码:321 / 327
页数:7
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